A curated catalogue of human genomic structural variation




Variant Details

Variant: nsv5501169



Internal ID278077
Landmark
Location Information
TypeCoordinatesAssemblyOther Links
chr11:56616791..56627916hg38UCSC Ensembl
chr11:56384267..56395392hg19UCSC Ensembl
Cytoband11q12.1
Allele length
AssemblyAllele length
hg3811126
hg1911126
Variant TypeCNV deletion
Copy Number
Allele State
Allele Origin
Probe Count
Validation Flag
Merged StatusM
Merged Variants
Supporting Variantsnssv17048233
Samples
Known Genes
MethodSequencing
Analysis
Platform
Comments
ReferenceByrska_Bishop_et_al_2022
Pubmed ID36055201
Accession Number(s)nsv5501169
Frequency
Sample Size3202
Observed Gain0
Observed Loss1
Observed Complex0
Frequencyn/a


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